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Tunable drug loading and release from polypeptide multilayer nanofilms

Polypeptide multilayer nanofilms were prepared using electrostatic layer-by-layer self-assembly nanotechnology. Small charged drug molecules (eg, cefazolin, gentamicin, and methylene blue) were loaded in polypeptide multilayer nanofilms. Their loading and release were found to be pH-dependent and co...

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Detalles Bibliográficos
Autores principales: Jiang, Bingbing, Li, Bingyun
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2720742/
https://www.ncbi.nlm.nih.gov/pubmed/19421369
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author Jiang, Bingbing
Li, Bingyun
author_facet Jiang, Bingbing
Li, Bingyun
author_sort Jiang, Bingbing
collection PubMed
description Polypeptide multilayer nanofilms were prepared using electrostatic layer-by-layer self-assembly nanotechnology. Small charged drug molecules (eg, cefazolin, gentamicin, and methylene blue) were loaded in polypeptide multilayer nanofilms. Their loading and release were found to be pH-dependent and could also be controlled by changing the number of film layers and drug incubation time, and applying heat-treatment after film formation. Antibioticloaded polypeptide multilayer nanofilms showed controllable antibacterial properties against Staphylococcus aureus. The developed biodegradable polypeptide multilayer nanofilms are capable of loading both positively- and negatively-charged drug molecules and promise to serve as drug delivery systems on biomedical devices for preventing biomedical device-associated infection, which is a significant clinical complication for both civilian and military patients.
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spelling pubmed-27207422009-08-31 Tunable drug loading and release from polypeptide multilayer nanofilms Jiang, Bingbing Li, Bingyun Int J Nanomedicine Original Research Polypeptide multilayer nanofilms were prepared using electrostatic layer-by-layer self-assembly nanotechnology. Small charged drug molecules (eg, cefazolin, gentamicin, and methylene blue) were loaded in polypeptide multilayer nanofilms. Their loading and release were found to be pH-dependent and could also be controlled by changing the number of film layers and drug incubation time, and applying heat-treatment after film formation. Antibioticloaded polypeptide multilayer nanofilms showed controllable antibacterial properties against Staphylococcus aureus. The developed biodegradable polypeptide multilayer nanofilms are capable of loading both positively- and negatively-charged drug molecules and promise to serve as drug delivery systems on biomedical devices for preventing biomedical device-associated infection, which is a significant clinical complication for both civilian and military patients. Dove Medical Press 2009 2009-04-01 /pmc/articles/PMC2720742/ /pubmed/19421369 Text en © 2009 Dove Medical Press Limited. All rights reserved
spellingShingle Original Research
Jiang, Bingbing
Li, Bingyun
Tunable drug loading and release from polypeptide multilayer nanofilms
title Tunable drug loading and release from polypeptide multilayer nanofilms
title_full Tunable drug loading and release from polypeptide multilayer nanofilms
title_fullStr Tunable drug loading and release from polypeptide multilayer nanofilms
title_full_unstemmed Tunable drug loading and release from polypeptide multilayer nanofilms
title_short Tunable drug loading and release from polypeptide multilayer nanofilms
title_sort tunable drug loading and release from polypeptide multilayer nanofilms
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2720742/
https://www.ncbi.nlm.nih.gov/pubmed/19421369
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